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PUBMED FOR HANDHELDS

Journal Abstract Search


112 related items for PubMed ID: 11918557

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  • 24. Familial pseudohyperkalemia: a rare cause of hyperkalemia.
    Sugimoto T, Kume S, Osawa N, Nakazawa J, Koya D, Kashiwagi A.
    Intern Med; 2005 Aug; 44(8):875-8. PubMed ID: 16157991
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  • 29. Possible screening test for familial pseudohyperkalaemia.
    Leadbeatter S, O'Dowd TC.
    Lancet; 1982 Jul 10; 2(8289):103-4. PubMed ID: 6123793
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  • 30. Hereditary stomatocytosis and cation-leaky red cells--recent developments.
    Bruce LJ.
    Blood Cells Mol Dis; 2009 Jul 10; 42(3):216-22. PubMed ID: 19261491
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  • 31. [Pseudo-hyperkalemia. Apropos of a familial case].
    Vantyghem MC, Dagher G, Doise B, Lallau G, Vandewalle B, Racadot A, Lefebvre J.
    Ann Endocrinol (Paris); 1991 Jul 10; 52(2):104-8. PubMed ID: 1929192
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  • 32. [Genetic diseases of erythrocyte membrane permeability].
    Delaunay J.
    Ann Biol Clin (Paris); 1999 Jul 10; 57(4):383-91. PubMed ID: 10432360
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  • 37. Allogeneic bone marrow transplantation for severe post-splenectomy thrombophilic state in leaky red cell membrane haemolytic anaemia of the stomatocytosis class.
    Bergheim J, Ernst P, Brinch L, Gore DM, Chetty MC, Stewart GW.
    Br J Haematol; 2003 Apr 10; 121(1):119-22. PubMed ID: 12670341
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  • 38. Hereditary disorders of potassium homeostasis.
    Warnock DG.
    Best Pract Res Clin Endocrinol Metab; 2003 Dec 10; 17(4):505-27. PubMed ID: 14687586
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  • 39. Missing band 7 membrane protein in two patients with high Na, low K erythrocytes.
    Lande WM, Thiemann PV, Mentzer WC.
    J Clin Invest; 1982 Dec 10; 70(6):1273-80. PubMed ID: 7174793
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  • 40. Familial pseudohyperkalemia: a rare syndrome, but diverse genetic heterogeneity.
    Kitamura K, Tomita K.
    Intern Med; 2005 Aug 10; 44(8):781-2. PubMed ID: 16157971
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